WO2020231924A1 - Indicateur coloré sensible au ph pour des applications de désinfection - Google Patents

Indicateur coloré sensible au ph pour des applications de désinfection Download PDF

Info

Publication number
WO2020231924A1
WO2020231924A1 PCT/US2020/032344 US2020032344W WO2020231924A1 WO 2020231924 A1 WO2020231924 A1 WO 2020231924A1 US 2020032344 W US2020032344 W US 2020032344W WO 2020231924 A1 WO2020231924 A1 WO 2020231924A1
Authority
WO
WIPO (PCT)
Prior art keywords
container
substrate
sensitive indicator
azo dye
red
Prior art date
Application number
PCT/US2020/032344
Other languages
English (en)
Inventor
Kaitlin Lake
Conor SMITH
Karl Heinbuch
Matthew Paul Molinaro
Original Assignee
Ecolab Usa Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ecolab Usa Inc. filed Critical Ecolab Usa Inc.
Priority to AU2020274035A priority Critical patent/AU2020274035B2/en
Priority to CN202080034554.7A priority patent/CN113811760B/zh
Priority to CN202411606159.8A priority patent/CN119460419A/zh
Priority to JP2021566479A priority patent/JP7282919B2/ja
Priority to EP20729457.0A priority patent/EP3953702A1/fr
Priority to MX2021013714A priority patent/MX2021013714A/es
Priority to EP22178057.0A priority patent/EP4083621B1/fr
Priority to BR112021022415-7A priority patent/BR112021022415B1/pt
Publication of WO2020231924A1 publication Critical patent/WO2020231924A1/fr

Links

Classifications

    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N31/00—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods
    • G01N31/22—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods using chemical indicators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
    • A61L2/26—Accessories or devices or components used for biocidal treatment
    • A61L2/28—Devices for testing the effectiveness or completeness of sterilisation, e.g. indicators which change colour
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/75—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
    • G01N21/77—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator
    • G01N21/78—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator producing a change of colour
    • G01N21/80—Indicating pH value
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D25/00—Details of other kinds or types of rigid or semi-rigid containers
    • B65D25/28—Handles
    • B65D25/2835—Swingable handles
    • B65D25/2852—Swingable handles provided on a local area near to or at the upper edge or rim
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D25/00—Details of other kinds or types of rigid or semi-rigid containers
    • B65D25/28—Handles
    • B65D25/2835—Swingable handles
    • B65D25/2855—Swingable handles centrally located in open container
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D25/00—Details of other kinds or types of rigid or semi-rigid containers
    • B65D25/54—Inspection openings or windows
    • B65D25/56—Inspection openings or windows with means for indicating level of contents
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N31/00—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods
    • G01N31/22—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods using chemical indicators
    • G01N31/226—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods using chemical indicators for investigating the degree of sterilisation

Definitions

  • the disclosure relates to pH sensitive indicators for sanitizing applications.
  • pH sensitive materials that indicate sufficient concentration of a sanitizing composition.
  • compositions including in particular sanitizing compositions
  • Various mechanisms have been employed to assess the concentration of the compositions largely focusing on measuring the active species. For example, in chlorine-based or quaternary ammonium-based compositions, the amount of chlorine or quaternary ammonium compound is often measured to assess whether the composition has a sufficient concentration for the particular cleaning application, e.g., sufficient to sanitize or disinfect.
  • the traditional mechanisms for measuring the concentration of the compositions suffer a number of drawbacks. For example, in some situations expensive test equipment is required to measure the concentrations.
  • Another drawback includes the need to analyze, interpret, and apply results to determine whether the active species concentration indicates a sufficient concentration for the particular application. Still another drawback is that the tests may not be able to provide real-time results regarding the concentration at an end use application. Finally, due to changes in stability of some components or equilibrium of chemistry, it has been necessary for personnel to test and assess the concentration of critical components in each bucket, sink, pail, or spray bottle prior to use to ensure the concentration is sufficient for the degree of cleaning, e.g., sanitizing or disinfecting.
  • Still a further object of the present disclosure is to provide a method and mechanism that provides concentration information in real-time, at a glance, without the need for analysis and interpretation.
  • pH sensitive color indicators disclosed herein provide a real-time indicator of the concentration of a cleaning composition.
  • Another advantage of the pH sensitive color indicators is that they provide a simple mechanism for determining whether an acceptable concentration of a sanitizing or disinfecting composition exists with a mechanism permitting an at-a-glance determination.
  • At least one embodiment disclosed herein comprises a distinct aesthetic appearance. Ornamental aspects included in such an embodiment can help capture a consumer’s attention and/or identify a source of origin of a product being sold. Said ornamental aspects will not impede functionality of the present invention.
  • a preferred embodiment, as described herein, comprises a pH sensitive indicator comprising an azo dye and a substrate; wherein the azo dye is bound to or coated on the substrate; wherein the azo dye exhibits a color change at a pH of about 4.5 or less.
  • a further embodiment, as described herein, comprises a method of detecting a concentration of a cleaning composition
  • a pH sensitive indicator comprises an azo dye and a substrate; wherein the azo dye is bound to or coated on the substrate; wherein the azo dye exhibits a color change at a pH of about 4.5 or less; wherein the substrate is a plastic, a metal, a textile, or cellulose based; determining whether the cleaning composition has a concentration efficacious for a cleaning application by observing whether the pH sensitive indicator exhibited a color change during or after the contacting step.
  • Another preferred embodiment, as described herein, comprises a method of cleaning a surface comprising contacting a cleaning composition with a pH sensitive indicator; wherein the pH sensitive indicator comprises an azo dye and a substrate; wherein the azo dye is bound to or coated on the substrate; wherein the azo dye exhibits a color change at a pH of about 4.5 or less; and wherein the substrate is a plastic, a metal, a textile, or cellulose based;
  • determining whether the cleaning composition has a low enough pH by observing whether the pH sensitive indicator exhibited a color change during or after the contacting step; and applying the cleaning composition to a surface if a color change was exhibited.
  • Figure 1 shows a rear, top perspective view of a pail with substantially transparent windows.
  • Figure 2 shows a front, top perspective view thereof.
  • Figure 3 shows an xz cross-sectional perspective view thereof.
  • Figure 4 shows an xy cross-section perspective view thereof.
  • Figure 5 shows a top elevational view thereof.
  • Figure 6 shows a bottom elevational view thereof.
  • Figure 7 shows a front elevational view thereof.
  • Figure 8 shows a rear elevational view thereof.
  • Figure 9 shows a left-side elevational view thereof.
  • Figure 10 shows a right-side elevational view thereof.
  • Figure 11 shows a rear perspective view of a substantially transparent pail.
  • Figure 12 shows a front perspective view thereof.
  • Figure 13 shows an xz cross-sectional perspective view thereof.
  • Figure 14 shows an xy cross-section perspective view thereof.
  • Figure 15 shows a top elevational view thereof.
  • Figure 16 shows a bottom elevational view thereof.
  • Figure 17 shows a front elevational view thereof.
  • Figure 18 shows a rear elevational view thereof.
  • Figure 19 shows a left-side elevational view thereof.
  • Figure 20 shows a right-side elevational view thereof.
  • Figure 21 shows a front, left-side perspective view of a substantially transparent pail with a substantially opaque sleeve and a plastic holder for a pH strip riveted thereto.
  • Figure 22 shows a rear, right-side perspective view thereof.
  • Figure 23 shows a front, top perspective view of a bucket comprising a window, which is shown as a non-limiting example of a substrate comprising pH sensitive indicator.
  • Figure 24 is a photograph of a cellulose-based sponge that has been modified to include an pH sensitive azo-dye via a covalent bonding mechanism which shows a color change where a cleaning composition has been applied to the sponge.
  • Figure 25 is a photograph of silica beads surface functionalized and bound to an exemplary pH sensitive azo dye in liquids at differing pHs to assess the color change of the silica.
  • Figure 26 is a photograph of different paint types (specifically water-based paints and oil-based paints) to assess the compatibility with pH sensitive azo dyes.
  • the present disclosure relates to pH sensitive color indicators for assessing the concentration of a cleaning composition, in particular, sanitizing and/or disinfecting compositions.
  • the disclosure also describes methods of making and using the pH sensitive color indicating products.
  • description of a range such as from 1 to 6 should be considered to have specifically disclosed sub-ranges such as from 1 to 3, from 1 to 4, from 1 to 5, from 2 to 4, from 2 to 6, from 3 to 6 etc., as well as individual numbers within that range, for example, 1, 2, 3, 4, 5, and 6, and decimals and fractions, for example, 1.2, 3.8, 1 1 ⁇ 2, and 4 3 ⁇ 4. This applies regardless of the breadth of the range.
  • the term“about,” as used herein, refers to variation in the numerical quantity that can occur, for example, through typical measuring techniques and equipment, with respect to any quantifiable variable, including, but not limited to, mass, volume, time, temperature, pH, and log count of bacteria or viruses. Further, given solid and liquid handling procedures used in the real world, there is certain inadvertent error and variation that is likely through differences in the manufacture, source, or purity of the ingredients used to make the compositions or carry out the methods and the like. The term“about” also encompasses these variations. Whether or not modified by the term“about,” the claims include equivalents to the quantities.
  • compositions of the present invention may comprise, consist essentially of, or consist of the components and ingredients of the present invention as well as other ingredients described herein.
  • “consisting essentially of’ means that the methods, systems, apparatuses and compositions may include additional steps, components or ingredients, but only if the additional steps, components or ingredients do not materially alter the basic and novel characteristics of the claimed methods, systems, apparatuses, and compositions.
  • actives or“percent actives” or“percent by weight actives” or“actives concentration” are used interchangeably herein and refers to the concentration of those ingredients involved in cleaning expressed as a percentage minus inert ingredients such as water or salts. It is also sometimes indicated by a percentage in parentheses, for example, “chemical (10%).”
  • alkyl or“alkyl groups” refers to saturated hydrocarbons having one or more carbon atoms, including straight-chain alkyl groups (e.g., methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, etc.), cyclic alkyl groups (or “cycloalkyl” or“alicyclic” or“carbocyclic” groups) (e.g., cyclopropyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, etc.), branched-chain alkyl groups (e.g., isopropyl, tert- butyl, sec-butyl, isobutyl, etc.), and alkyl-substituted alkyl groups (e.g., alkyl-substituted
  • the term“alkyl” includes both“unsubstituted alkyls” and “substituted alkyls.”
  • the term“substituted alkyls” refers to alkyl groups having substituents replacing one or more hydrogens on one or more carbons of the hydrocarbon backbone. Such substituents may include, for example, alkenyl, alkynyl, halogeno, hydroxyl, alkylcarbonyloxy, arylcarbonyloxy, alkoxycarbonyloxy, aryloxy, aryloxycarbonyloxy, carboxylate, alkylcarbonyl, arylcarbonyl, alkoxycarbonyl,
  • aminocarbonyl alkylaminocarbonyl, dialkylaminocarbonyl, alkylthiocarbonyl, alkoxyl, phosphate, phosphonato, phosphinato, cyano, amino (including alkyl amino, dialkylamino, arylamino, diarylamino, and alkylarylamino), acylamino (including alkylcarbonylamino, arylcarbonylamino, carbamoyl and ureido), imino, sulfhydryl, alkylthio, arylthio, thiocarboxylate, sulfates, alkylsulfinyl, sulfonates, sulfamoyl, sulfonamido, nitro, trifluoromethyl, cyano, azido, heterocyclic, alkylaryl, or aromatic (including heteroaromatic) groups.
  • substituted alkyls can include a heterocyclic group.
  • heterocyclic group includes closed ring structures analogous to carbocyclic groups in which one or more of the carbon atoms in the ring is an element other than carbon, for example, nitrogen, sulfur or oxygen. Heterocyclic groups may be saturated or unsaturated.
  • heterocyclic groups include, but are not limited to, aziridine, ethylene oxide (epoxides, oxiranes), thiirane (episulfides), dioxirane, azetidine, oxetane, thietane, dioxetane, dithietane, dithiete, azolidine, pyrrolidine, pyrroline, oxolane, dihydrofuran, and furan.
  • aziridine ethylene oxide (epoxides, oxiranes), thiirane (episulfides), dioxirane, azetidine, oxetane, thietane, dioxetane, dithietane, dithiete, azolidine, pyrrolidine, pyrroline, oxolane, dihydrofuran, and furan.
  • soil refers to any soil, including, but not limited to, non-polar oily and/or hydrophobic substances which may or may not contain particulate matter such as industrial soils, mineral clays, sand, natural mineral matter, carbon black, graphite, kaolin, environmental dust, and/or food based soils such as blood, proteinaceous soils, starchy soils, fatty soils, cellulosic soils, etc.
  • non-polar oily and/or hydrophobic substances which may or may not contain particulate matter such as industrial soils, mineral clays, sand, natural mineral matter, carbon black, graphite, kaolin, environmental dust, and/or food based soils such as blood, proteinaceous soils, starchy soils, fatty soils, cellulosic soils, etc.
  • the term“antimicrobial” refers to a compound or composition that reduces and/or inactivates a microbial population, including, but not limited to bacteria, viruses, fungi, and algae within about 10 minutes or less, about 8 minutes or less, about 5 minutes or less, about 3 minutes or less, about 2 minutes or less, about 1 minute or less, or about 30 seconds or less.
  • the term antimicrobial refers to a composition that provides at least about a 3-log, 3.5 log, 4 log, 4.5 log, or 5 log reduction of a microbial population in about 10 minutes or less, about 8 minutes or less, about 5 minutes or less, about 3 minutes or less, about 2 minutes or less, about 1 minute or less, or about 30 seconds or less.
  • sanitizer refers to an agent that reduces the number of bacterial contaminants to safe levels as judged by public health requirements.
  • sanitizers for use in this invention will provide at least a 99.999% reduction (5- log order reduction). These reductions can be evaluated using a procedure set out in
  • sanitizer should provide a 99.999% reduction (5-log order reduction) within 30 seconds at room temperature, 25 ⁇ 2°C, against several test organisms.
  • the term“cleaning” refers to a method used to facilitate or aid in soil removal, bleaching, microbial population reduction, and any combination thereof.
  • the term“microorganism” refers to any noncellular or unicellular (including colonial) organism. Microorganisms include all prokaryotes. Microorganisms include bacteria (including cyanobacteria), spores, lichens, fungi, protozoa, virinos, viroids, viruses, phages, and some algae.
  • the term“microbe” is synonymous with microorganism.
  • the phrase“food processing surface” refers to a surface of a tool, a machine, equipment, a structure, a building, or the like that is employed as part of a food processing, preparation, or storage activity.
  • Examples of food processing surfaces include surfaces of food processing or preparation equipment (e.g., slicing, canning, or transport equipment, including flumes), of food processing wares (e.g., utensils, dishware, wash ware, and bar glasses), and of floors, walls, or fixtures of structures in which food processing occurs.
  • Food processing surfaces are found and employed in food anti-spoilage air circulation systems, aseptic packaging sanitizing, food refrigeration and cooler cleaners and sanitizers, ware washing sanitizing, blancher cleaning and sanitizing, food packaging materials, cutting board additives, third-sink sanitizing, beverage chillers and warmers, meat chilling or scalding waters, autodish sanitizers, sanitizing gels, cooling towers, food processing antimicrobial garment sprays, and non-to-low-aqueous food preparation lubricants, oils, and rinse additives.
  • hard surface refers to a solid, substantially non-flexible surface such as a counter top, tile, floor, wall, panel, window, plumbing fixture, kitchen and bathroom furniture, appliance, engine, circuit board, dish, mirror, window, monitor, touch screen, and thermostat.
  • Hard surfaces are not limited by the material; for example, a hard surface can be glass, metal, tile, vinyl, linoleum, composite, wood, plastic, etc. Hard surfaces may include for example, health care surfaces and food processing surfaces.
  • health care surface refers to a surface of an instrument, a device, a cart, a cage, furniture, a structure, a building, or the like that is employed as part of a health care activity.
  • health care surfaces include surfaces of medical or dental instruments, of medical or dental devices, of electronic apparatus employed for monitoring patient health, and of floors, walls, or fixtures of structures in which health care occurs. Health care surfaces are found in hospital, surgical, infirmity, birthing, mortuary, and clinical diagnosis rooms.
  • These surfaces can be those typified as“hard surfaces” (such as walls, floors, bed-pans, etc.,), or fabric surfaces, e.g., knit, woven, and non-woven surfaces (such as surgical garments, draperies, bed linens, bandages, etc.,), or patient-care equipment (such as respirators, diagnostic equipment, shunts, body scopes, wheel chairs, beds, etc.,), or surgical and diagnostic equipment.
  • Health care surfaces include articles and surfaces employed in animal health care.
  • instrument refers to the various medical or dental instruments or devices that can benefit from cleaning with a composition according to the present invention.
  • the phrases“medical instrument,”“dental instrument,”“medical device,”“dental device,”“medical equipment,” or“dental equipment” refer to instruments, devices, tools, appliances, apparatus, and equipment used in medicine or dentistry. Such instruments, devices, and equipment can be cold sterilized, soaked or washed and then heat sterilized, or otherwise benefit from cleaning in a composition of the present invention.
  • These various instruments, devices and equipment include, but are not limited to: diagnostic instruments, trays, pans, holders, racks, forceps, scissors, shears, saws (e.g. bone saws and their blades), hemostats, knives, chisels, rongeurs, files, nippers, drills, drill bits, rasps, burrs, spreaders, breakers, elevators, clamps, needle holders, carriers, clips, hooks, gouges, curettes, retractors, straightener, punches, extractors, scoops, keratomes, spatulas, expressers, trocars, dilators, cages, glassware, tubing, catheters, cannulas, plugs, stents, scopes (e.g., endoscopes, stethoscopes, and arthroscopes) and related equipment, and the like, or combinations thereof.
  • diagnostic instruments trays, pans, holders, racks, forceps, scissors, shears, saws (
  • microorganism refers to any noncellular or unicellular (including colonial) organism. Microorganisms include all prokaryotes. Microorganisms include bacteria (including cyanobacteria), spores, lichens, fungi, protozoa, virinos, viroids, viruses, phages, and some algae. As used herein, the term“microbe” is synonymous with microorganism.
  • soft surface refers to surfaces not classified as hard surfaces, but which are solid surfaces.
  • Soft surfaces include, but are not limited to, textiles, fabrics, woven surfaces, and non-woven surfaces.
  • Soft surfaces include, but are not limited to, carpet, curtains, fabrics, hospital partitions, linens, and upholstery.
  • the term“substantially free” refers to compositions completely lacking the component or having such a small amount of the component that the component does not affect the performance of the composition.
  • the component may be present as an impurity or as a contaminant and shall be less than 0.5 wt-%. In another embodiment, the amount of the component is less than 0.1 wt-% and in yet another embodiment, the amount of component is less than 0.01 wt-%.
  • virus refers to a type of microorganism that can include both pathogenic and non-pathogenic viruses.
  • Pathogenic viruses can be classified into two general types with respect to the viral structure: enveloped viruses and non-enveloped viruses.
  • enveloped viruses include herpes virus, influenza virus;
  • Non-enveloped viruses include the families Picomaviridae, Reoviridae, Caliciviridae, Adenoviridae and Parvoviridae. Members of these families include rhinovirus, poliovirus, adenovirus, hepatitis A virus, norovirus, papillomavirus, and rotavirus. It is known in the art that“enveloped” viruses are relatively sensitive and, thus, can be inactivated by commonly used disinfectants.
  • non-enveloped viruses are substantially more resistant to conventional disinfectants and are significantly more environmentally stable than enveloped viruses.
  • the term“ware” refers to items such as eating and cooking utensils, dishes, and other hard surfaces such as showers, sinks, toilets, bathtubs, countertops, windows, mirrors, transportation vehicles, and floors.
  • the term“ware” refers to items such as eating and cooking utensils, dishes, and other hard surfaces such as showers, sinks, toilets, bathtubs, countertops, windows, mirrors, transportation vehicles, and floors.
  • the term“ware” refers to items such as eating and cooking utensils, dishes, and other hard surfaces such as showers, sinks, toilets, bathtubs, countertops, windows, mirrors, transportation vehicles, and floors.
  • warewashing refers to washing, cleaning, or rinsing ware. Ware also refers to items made of plastic.
  • Types of plastics that can be cleaned with the compositions according to the invention include but are not limited to, those that include polypropylene polymers (PP), polycarbonate polymers (PC), melamine formaldehyde resins or melamine resin (melamine), acrylonitrile-butadiene-styrene polymers (ABS), and polysulfone polymers (PS).
  • Other exemplary plastics that can be cleaned using the compounds and compositions of the invention include polyethylene terephthalate (PET) polystyrene polyamide.
  • water soluble and“water dispersible” as used herein, means that the ingredient is soluble or dispersible in water in the inventive compositions.
  • the ingredient should be soluble or dispersible at 25° C concentration of between about 0.1 wt.% and about 15 wt.% of the water, more preferably at a concentration of between about 0.1 wt.% and about 10 wt.%.
  • weight percent refers to the concentration of a substance as the weight of that substance divided by the total weight of the composition and multiplied by 100.
  • the present disclosure relates to pH sensitive color indicators for assessing the concentration of a cleaning composition, in particular, sanitizing and/or disinfecting compositions.
  • the disclosure also describes methods of making and using the pH sensitive color indicating products.
  • acid anionic cleaning compositions we have found that the necessary concentration of active ingredient in acid anionic cleaners can be evaluated by determining the pH of a composition, which is related to the concentration of the active ingredient.
  • pH sensitive color indicators do currently exist, those in existence suffer many problems making them difficult to use. For example, existing pH sensitive color indicators are require immersion (of a test strip) or addition (of a use solution) to a vial of test chemical for a set amount of time such as 5 seconds, required reading of the result within 10 seconds at a set temperature, and a required comparison to a standard where colors and hues must be compared within that 10 second period before the results may no longer be viable. Such methods are difficult to employ in the field due to differences in conditions such as temperature and the requirement that results be read and determined within set amounts of time. Further, such methods are irreversible and thus not continual and in real-time where changes to the compositions can be readily monitored over a time period without the need to retest.
  • pH sensitive color indicator By using a pH sensitive color indicator, the need for expensive and/or complicated equipment used to measure the active cleaning components in a composition (such as chlorine or quaternary ammonium) are not necessary. Further, there is no need to analyze and interpret test results to evaluate the suitability of a particular concentration. Rather the use of pH sensitive color indicators can provide an image or color change at-a- glance to signal that a concentration is sufficient or insufficient for the desired cleaning application, i.e., whether the concentration is sufficient for sanitizing or disinfecting.
  • the pH sensitive color indicators comprise a pH sensitive dye bound to a substrate to allow for visual indication of the concentration of a cleaning composition.
  • a color change or appearance of an image can indicate that a composition is either in or out of the required concentration to achieve a particular antimicrobial activity.
  • the pH sensitive color indicators can provide an at-a-glance real-time determination of a composition’s sanitizing and/or disinfecting efficacy.
  • the pH sensitive color indicator can comprise a dye and a substrate.
  • the pH sensitive color indicators comprise a pH sensitive dye.
  • the dye comprises an azo dye.
  • the dye employed can be a combination or mixture of dyes including mixtures comprised of two azo dyes, three azo dyes, four azo dyes, or more.
  • Azo dyes are organic compounds comprising one or more diazenyl functional groups:
  • R and R' are either an aryl group or an alkyl group.
  • Preferred azo dyes include those where R has between 2 and 20 carbons, more preferably between 4 and 16 carbons, and where R' has between 2 and 20 carbons, more preferably between 4 and 16 carbons.
  • suitable azo dyes see U.S. Patent No. 4,029,598 at column 2, line 7 through column 5, line 68, which is incorporated herein by reference in its entirety.
  • Preferred azo dyes include, but are not limited to, allura red AC, azo violet, basic red 18, bromothymol blue, Congo red, direct blue 1, direct brown 78, m-cresol purple, methyl orange, methyl red, para red, phenol red, reactive orange 16, tartrazine, thymol blue, xylenol blue, xylenol orange, and combinations or mixtures thereof.
  • the pH sensitive dye exhibits a color change at a pH of about 4.5 or less, at about 4.4 or less, at about 4.3 or less, at about 4.2 or less, at about 4.1 or less, about 4 or less, at about 3.9 or less, at about 3.8 or less, at about 3.7 or less, at about 3.6 or less, at about 3.5 or less, at about 3.4 or less, at about 3.2 or less, at about 3.1 or less, at about 3.0 or less, at about 2.9 or less, at about 2.8 or less, at about 2.7 or less, at about 2.6 or less, at about 2.5 or less, at about 2.4 or less, at about.
  • the pH sensitive dye exhibits a color change at a pH between about 2 and about 4.5, more preferably between about 2.2 and about 4.0, still more preferably between about 2.5 and about 3.5, or most preferably at a pH between about 2.8 and about 3.2.
  • the pH sensitive dye has a pKa between about 2 and about 4.5, more preferably between about 2.2 and about 4, most preferably between about 2.5 and about 3.5.
  • the azo dye is bound to or coated on a substrate such that in contact with a cleaning composition, the azo dye can change color on the substrate to indicate a sufficient or insufficient concentration for antimicrobial efficacy.
  • the substrate can be any suitable substrate for a particular cleaning application.
  • the substrate can be, but is not limited to, a pail, a bucket, a dispenser, a spray bottle, a sprayer, a trigger sprayer, a sink, a coating, a liner, a mop, a paint, a paper, a sponge, a sticker, a towel, a window, or a wipe.
  • the azo dye can be bound to or coated on the substrate.
  • the substrate can be a paper having the azo dye bound or coated such that the dye exhibits a color change on the paper.
  • the substrate can be adhered (or otherwise affixed) to a surface, wherein the surface is one or more of a plastic surface, a composite surface, a glass surface, or a metal surface.
  • the azo dye is bound to or coated on a cellulose-based substrate, wherein the cellulose-based substrate is adhered (or otherwise affixed) to a surface, and wherein that surface is removably attached to a container, a pail, a bucket, a dispenser, a bottle, a sprayer, or a sink.
  • Figures 1-23 show non-limiting example embodiments of a substrate comprising a container 100, such as a pail or bucket.
  • the container 100 typically includes a base 102, sidewall(s) 104, and an upper rim 106.
  • the external side of the base 102 acts as the surface through which the pail or bucket 100 can operatively rest on external surface(s).
  • the base 102 can optionally include feet, to decrease the surface area in contact with said external surface(s).
  • the at least one sidewall 104 forms an upstanding boundary about the
  • the at least one sidewall 104 can include sections having varying tapers relative to a vertical plane.
  • an upper portion of the container 100 can include a greater outward taper relative to vertical than the lower portion of the container 100, and the upper rim 106 of the container 100 can be configured to have a taper relative to vertical greater than the upper and lower portions.
  • the sidewall 104 can extend generally upwardly and outwardly to flare near the mouth of the container 100 to aid in minimizing the amount of fluid spilled when filling the container 100 and to direct fluid from the bucket during pouring.
  • the sidewall 104 and base 102 together may preferably form a substantially cylindrical shape, however can be configured so as to take on any suitable or otherwise known three-dimensional shape.
  • the shape of the container 100 can be selected from the group consisting of cylinders, ellipsoids (including spheres), partial ellipsoids (including hemispheres), regular polyhedrons (including pyramids, cubes, etc.), irregular polyhedrons, cones, combinations thereof, and/or the like.
  • the container 100 is preferably constructed from materials such a polypropylene for withstanding handling of the chemistries disclosed herein. Other thermoplastics, such as those commonly used in injection molding processes, can also be used.
  • the sidewall 104 and base 102 may be solid, partially hollow, or mostly hollow, but should at least be thick enough to establish a sufficient strength for the container 100 so as to withstand impacts and abrasion over the course of repeated use.
  • the container 100 of Figures 1-10 includes a two-material design wherein most of the pail or bucket 100 is opaque and a minority portion, e.g. windows 108, 110 of the pail or bucket 100 is transparent.
  • Suitable transparent materials for the windows 108, 110 can non- limitingly include glass, fiberglass, polycarbonates, and/or the like.
  • the windows 108 and 110 permit wide viewing angles into the container 100 from external locations.
  • a pH strip 112 having the advantages disclosed herein and/or labels identifying the chemistries contained within the container 100 may be placed between the flexible retaining arms 114 and one or more of the windows 108, 110.
  • the flexible retaining arms 114 are rigid enough so as to secure the pH strip and/or labels in position during movement of the bucket, but should be deformable enough so as to allow users to remove and/or replace pH strips and/or labels between uses of the container 100, and so as to accommodate pH strips and/or labels of varying thicknesses.
  • the pH strip 112 and/or product identifiers may be stored at a location adjacent the windows 108, 110 until placed the interior of the sidewall 104 of the container 100.
  • the user will be able to view the pH strip 112 and/or product identifier inside the container 100 without having to see through the top of the same.
  • an upper holder 116 is positioned on the interior or uppermost portion of the sidewall 104 so as to stabilize the pH strip 112 while inserted into one or more of the retention arms 114 extending from a location just above where the sidewall 104 meets the base 102 of the container 100.
  • the retaining arms 114 substantially extend from a location just above the base 102 to the upper holder 116 and provide a retention area between the retention arms 114 and the window 108, 110, where the pH strip 112 can be slid therebetween.
  • the pH strip 112 can be slid into a position for viewing from a upward location and in a downward direction, can be slid into position laterally, and/or a combination of the aforementioned directions.
  • Such a slidable connection can be established through the use of one or more suitable slidable elements, including: a friction fit on a slip (non-stick) surface, guides, tracks, piston(s), shaft(s), sleeve(s), collar(s), ball bearings, actuator(s), linkage(s), pivot(s), and/or the like. It is preferred that the slidable connection only allow the pH strip 112, retention arms 114, and/or upper holder 116 to slide in one dimension (i.e. linearly) with respect to the sidewall 104. Yet, it is to be appreciated some minor relief in a second dimension can be to mitigate wear, tear, or failure of slidable components and/or elements. To that end, oils, grease, lubricants, antistatic agents, and/or other non-viscous fluids or devices can be applied where wear and tear is expected to further mitigate the same over time.
  • the retention arms 114 exert a force generally directed towards the window 108, 110, the force may be easily overcome by a user to slide the pH strip 112 between the retention arms 114 and window.
  • the retention arms 38 include some elasticity to re exert tension to press the badge in place.
  • the retention arm 114 / upper holder 116 combination may be fastened or otherwise affixed to the sidewall 104 by rivets 118. Other methods and means of attaching the retention arm 114 / upper holder 116 combination to the container 100 are also contemplated to be part of the invention.
  • the retention arm 114 / upper holder 116 combination may be adhered or otherwise secured to the container 100 via adhesives, screws, snaps, Velcro®, and/or the like. It is also contemplated that the retention arm 114 / upper holder 116 combination be molded or otherwise formed as part of the base 102 and/or sidewall 104 such that it is integrally one piece with the container 100. Therefore, the retention arm 114 / upper holder 116
  • combination may comprise a material similar to the dispenser body, such as a thermoplastic or the like.
  • the upper rim 106 of the container 100 can be reinforced with any number of intermediate support members 120.
  • the intermediate support members bridge the sidewall 104 and a lower and outward portion of the upper rim 106.
  • the upper rim 106 of the container 10 can curve downwardly and outwardly so as to be gripped by a user.
  • Opposing portions of sidewall(s) 104 of the container 100 include ears 122 with apertures 123 positioned generally at the middle of the sidewall 104 and approximate the mouth of the container 100.
  • the ears 122 can be positioned closer to the center of gravity of the container 100 to lessen the strain on the user when pouring liquids from the
  • each ear 122 is configured to receive posts 130 and 132 on respective ends 126 and 128 of the bail 124 as best illustrated in Figures 21-22.
  • the posts 130 and 132 may be removably attached to the ears 122 on the container, or in a few embodiments, permanently attached thereto. It is preferred the posts 130 and 132 are pivotally attached to ears 122 via the apertures 123 on the container 100 which allows the bale 124 to pivot about the ears.
  • the bale 124 is permitted to freely rotate at least 180°, such as from an upstanding position to adjacent either sidewall 104 to any point therebetween.
  • Mechanisms may be included on the container 100 so as to allow the bale 124 to be moved into pre-set interval positions such that the bail 124 cannot be dislodged therefrom unless the same mechanism or some other mechanism ( e.g . a lock) is disabled or enough force is applied to the bale 124 to overcome the biasing force of the included mechanisms.
  • the bale 124 is generally semicircular in shape and can optionally include a handle at the central, upper portion of an arc forming the semicircular shape.
  • product source identifiers 134 liquid volume indicators 136, instructions for use 138, a legend 140 for the pH strip 112 (shown in Figures 21-23), and/or universal hazard symbols 142 can be made integral with and/or placed on the sidewalls 104 of the container 100 to facilitate quick identification of aspects related to the container 100 and/or the liquid intended to be stored and/or handled therein and/or dispensed therefrom, such as a sanitizer or other suitable cleaning agent. It is thus within the scope of the present invention that source identifiers, indicia, caution symbols, instructions, and/or other desirable identifying information made up of letters, numbers, graphics, markings, and/or other symbols be printed on the container 100.
  • any suitable process for doing so that is compatible with the material that the container 100 is manufactured of such as a silk screen or photolithograph process or the like can be used.
  • the indicia, instructions, and/or other identifying information can be raised (embossed), depressed, stamped, etched, written, labeled, painted, coated, or otherwise applied to internal and/or external portions of the base 102 and/or sidewall 104. Indicia can be applied to planar and non-planar surfaces.
  • the pH strip 112 and any azo dye contained therein can be bound to a number of different places which can be observed.
  • the azo dye can be bound to the interior of the bucket or pail 100 and viewed through the window 108, 110.
  • the bucket or pail 100 can be painted with a paint comprising the azo dye
  • the bucket material itself can have the azo dye bound to it
  • a sticker can be added to the interior of the bucket or pail 100 wherein the sticker comprises the azo dye
  • another object such as a plastic coupon, disc, or float comprising the azo dye or containing paint comprised of azo dye could be affixed to the bucket or pail 100, or the window can comprise the bound azo dye.
  • the substrate can be coated and/or painted with a composition comprising the pH sensitive dye.
  • the pH sensitive dye is in a non water soluble paint, which is applied to a substrate.
  • the visual appearance of the pH strip 112 may thus be designed to aid in
  • the pH strip 112 may be configured to show a color or several colors which contrast or are compatible with color(s) of adjacent object(s).
  • the colors revealed may for example, comprise a primary color, secondary color, tertiary color, or any combination thereof.
  • the colors of the pH strip 112 can convey a particular meaning to a user. Caution might be indicated by a redder color and a warning may become visible if the pH falls out of a desirable range. A more uniform blue or green color might indicate a good solution. If the pH increases, the pH strip 112 may have more of a pinkish color.
  • a substrate used to apply a cleaning composition can comprise the bound azo dye.
  • a paper, a wipe, a towel, a sponge, a sprayer, a trigger sprayer, or a mop can comprise a bound azo dye.
  • Suitable substrates can include, but are not limited to, plastics, metals, cellulose-based, or textiles.
  • the substrate once in contact with the cleaning composition can provide an indication as to whether the composition is efficacious for the particular cleaning application.
  • the methods and techniques of preparing pH indicators can be produced in several ways, such as those described in U.S. Patent No. 4,029,598 which is incorporated herein by reference in its entirety.
  • Such techniques utilize a carrier, such as cellulose, and saturate the carrier with azo dyes having reactive groups capable of forming a chemical bond with the carrier material to form pH indicators that do not bleed.
  • the methods include directly coloring a substrate, such as indicator paper comprising cellulose fibers during the manufacture thereof, by first suspending the paper raw material with water in suitable beaters, mixing the resultant suspension with an aqueous solution of the dye, and then making the suspension alkaline by the addition of bases for fixing the dye on the fiber.
  • a second method involves imprinting a finished substrate, such as indicator paper, with a dye solution and fixing the dyes by a brief immersion into a warm alkaline fixing solution.
  • the dye solution can be applied to a paper previously made alkaline, which after the application of the dye solution and a subsequent brief treatment in steam, is washed neutral and dried.
  • the pH sensitive dye is bound to the substrate in an amount between about 0.01 to about 0.1 grams of dye per 10 grams of bindable surface area of substrate.
  • the azo dye can comprise a fixative. Suitable fixatives include, but are not limited to, salts, acids, or bases.
  • the pH sensitive dye can be used to indicate a positive or negative result regarding the efficacy of a cleaning composition for a desired application.
  • the pH indicator can change color to indicate that a cleaning composition has a pH at or below a maximum pH level for the efficacy of a particular antimicrobial activity such as sanitizing or disinfecting.
  • an azo dye can be selected which exhibits a color change at a pH of about 3.2; this way if a composition has a pH of 3.2 or lower (i.e., it is efficacious for its particular application), it will change the color of the dye bound to the substrate indicating its efficacy; alternatively, if the cleaning composition is above 3.2 and not efficacious for its intended antimicrobial efficacy the color change will not be present when the composition is in contact with the pH sensitive dye.
  • the dye can be bound to the substrate in a pattern to reveal an image which signals a low enough pH for the composition to be efficacious.
  • the color itself is not critical but rather the revealing of the pattern or image.
  • a preferred embodiment comprises a method of detecting a concentration of a cleaning composition.
  • the method can comprise contacting a cleaning composition with a pH sensitive indicator and determining whether the cleaning composition has a concentration efficacious for a cleaning application by observing whether the pH sensitive indicator exhibited a color change during or after the contacting step.
  • a preferred embodiment comprises a method of cleaning a surface.
  • the method can comprise contacting a cleaning composition with a pH sensitive indicator and determining whether the cleaning composition has a concentration efficacious for a cleaning application by observing whether the pH sensitive indicator exhibited a color change during or after the contacting step and applying the cleaning composition to a surface if a color change was exhibited.
  • the cleaning can be sanitizing or disinfecting the surface. If the composition does not affect a color change to the pH indicator, then the cleaning composition can be modified by adjusting the pH.
  • the pH can be adjusted by increasing the concentration of the active cleaning composition components and/or by adding a pH modifier.
  • the compositions provide at least about a 3-log reduction of a microbial population, more preferably at least about a 3.5 -log reduction, still more preferably equal to or greater than about 4-log reduction, even more preferably equal to or greater than about 4.5-log reduction, and most preferably equal to or greater than about 5-log reduction.
  • the cleaning compositions provide these reductions in about 30 minutes or less, about 20 minutes or less, about 15 minutes or less, about 10 minutes or less, about 5 minutes or less, about 4 minutes or less, about 3 minutes or less, about 2 minutes or less, about 90 seconds or less, about 60 seconds or less, even about 30 seconds or less.
  • the cleaning compositions compatible with the pH sensitive indicators are those having efficacy at a pH equal to or below about 4.5, more preferably equal to or below about 4, more preferably equal to or below about 3.5, still more preferably equal to or below about 3.2, yet more preferably equal to or less than about 3.0, and even more preferably equal to or less than about 2.8.
  • compositions can include peracid compositions, acid anionic compositions, or combinations or mixtures thereof.
  • the cleaning composition comprises at least one anionic sulfonated or sulfated surfactant.
  • the desired concentration for sanitizing or disinfecting is between about 5 ppm and about 6000 ppm, more preferably between about 15 ppm and about 5000 ppm, and most preferably between about 100 ppm and about 4500 ppm.
  • the pH is preferably equal to or less than about 3.2, equal to or less than about 3.1, equal to or less than about 3.0, equal to or less than about 2.9, equal to or less than about 2.8.
  • Anionic surfactants are surface active substances which are categorized by the negative charge on the hydrophile; or surfactants in which the hydrophilic section of the molecule carries no charge unless the pH is elevated to the pKa or above (e.g. carboxylic acids).
  • Carboxylate, sulfonate, sulfate and phosphate are the polar (hydrophilic) solubilizing groups found in anionic surfactants.
  • sodium, lithium and potassium impart water solubility; ammonium and substituted ammonium ions provide both water and oil solubility; and, calcium, barium, and magnesium promote oil solubility.
  • Preferred anionic sulfonated surfactants include alkyl sulfonates, the linear and branched primary and secondary alkyl sulfonates, and the aromatic sulfonates with or without substituents.
  • sulfonates include sulfonated carboxylic acid esters.
  • suitable alkyl sulfonate surfactants include C8-C22 alkylbenzene sulfonates, or C10-C22 alkyl sulfonates.
  • the anionic alkyl sulfonate surfactant is linear alkyl benzene sulfonic acid (LAS).
  • the compositions are most effective at pH 3.5 or below.
  • the anionic sulfonate surfactant may alternatively or additionally include diphenylated sulfonates, and/or sulfonated oleic acid.
  • anionic sulfonated surfactants include, but are not limited to, C8-C22 alkylbenzene sulfonates, sulfonated oleic acid, a sulfosuccinate, a secondary alkane sulfonate, or mixtures thereof.
  • the antimicrobial multi-purpose compositions of the present application may be substantially or entirely free of other surfactants including, amphoteric surfactants, cationic surfactants, nonionic surfactants, zwitterionic surfactants, or other anionic surfactants.
  • the compositions can optionally comprise a buffering agent.
  • the composition employs a pH buffering agent with a pKa between about 2 and about 3. If a buffering agent is included in the compositions, it can be in any suitable amount to buffer the composition at a desired pH.
  • the concentrated antimicrobial multi-purpose composition comprises between about 0 wt.% and about 20 wt.%, more preferably between about 0.01 wt.% and about 15 wt.%, and most preferably between about 0.01 wt.% and about 10 wt.% of a buffering agent.
  • the ready-to-use antimicrobial multi-purpose composition comprises between about 0 wt.% and about 3 wt.%, more preferably between about 0.01 wt.% and about 3 wt.%, and most preferably between about 0.01 wt.% and about 3 wt.% of a buffering agent.
  • the buffering agent is in an amount less than about 0.5 wt.%, more preferably less than about 0.1 wt.%.
  • Preferred buffering agents include, but are not limited to, phosphonates, phosphonic acids, and/or phosphates.
  • Exemplary buffering agents include a phosphonate salt(s) and/or a heterocyclic dicarboxylic acid, e.g., dipicolinic acid.
  • the buffering agent is pyridine carboxylic acid-based stabilizers, such as picolinic acid and salts, pyridine- 2, 6-dicarboxylic acid and salts, and phosphonate-based stabilizers, such as phosphoric acid and salts, pyrophosphoric acid and salts and most commonly 1 -hydroxy ethylidene- 1,1- diphosphonic acid (HEDP) and salts.
  • HEDP 1 -hydroxy ethylidene- 1,1- diphosphonic acid
  • compositions and methods can comprise two or more buffering agents, e.g., HEDP and 2,6-pyridinedicarboxylic acid (DP A).
  • buffering agents include, but are not limited to, triethanol amine, imidazole, a carbonate salt, a phosphate salt, heterocyclic carboxylic acids, phosphonates, etc.
  • the composition is free of a carboxylic acid buffering agent.
  • the compositions can optionally include one or more pH modifiers to adjust pH and/or neutralize other ingredients.
  • an alkaline pH modifier is added as an alkalizing agent.
  • an alkaline pH modifier is added to compositions comprising no chelant or a non-neutralized chelant.
  • an acidic pH modifier is added to compositions comprising a neutralized chelant.
  • an acidic pH modifier can be added as a coacidulant for disinfecting applications.
  • the concentrated antimicrobial multi purpose composition comprises between about 0 wt.% and about 10 wt.%, more preferably between about 0.01 wt.% and about 8 wt.%, and most preferably between about 0.01 wt.% and about 5 wt.% of a pH modifier.
  • the ready-to-use composition comprises between about 0 wt.% and about 10 wt.%, more preferably between about 0.01 wt.% and about 8 wt.%, and most preferably between about 0.01 wt.% and about 5 wt.% of a pH modifier.
  • the ready-to-use comprises between about 0 wt.% and about 10 wt.%, more preferably between about 0.01 wt.% and about 8 wt.%, and most preferably between about 0.01 wt.% and about 5 wt.% of a pH modifier.
  • the ready-to-use composition comprises between about 0 wt.% and about 10 wt.%,
  • antimicrobial multi-purpose composition comprises between about 0 wt.% and about 10 wt.%, more preferably between about 0.01 wt.% and about 5 wt.%, and most preferably between about 0.01 wt.% and about 3 wt.% of a pH modifier.
  • Alkaline pH modifier preferably between about 0.01 wt.% and about 5 wt.%, and most preferably between about 0.01 wt.% and about 3 wt.% of a pH modifier.
  • compositions may include one or more alkaline pH modifiers to adjust the compositions to a desired pH.
  • Suitable alkaline pH modifiers include, but are not limited to, one or more organic alkaline pH modifiers, one or more inorganic alkaline pH modifiers, or combinations thereof.
  • Suitable organic alkaline pH modifiers include, but are not limited to, amines and strong nitrogen bases including, for example monoethanolamine, monopropanolamine,
  • Suitable inorganic alkaline pH modifiers include, but are not limited to, alkali metal hydroxides (e.g. sodium hydroxide, potassium hydroxide, or the like, or combinations thereof), alkali metal carbonates (e.g., sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate, sodium sesquicarbonate, potassium sesquicarbonate, and the like, or combinations thereof), alkali metal borates (e.g., sodium borate, potassium borate, and the like, or combinations thereof), alkali metal oxides (e.g., sodium oxide, potassium oxide, and the like, or combinations thereof), and the like, or combinations thereof.
  • alkali metal hydroxides e.g. sodium hydroxide, potassium hydroxide, or the like, or combinations thereof
  • alkali metal carbonates e.g., sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate, sodium sesquicarbonate, potassium sesquicarbonate, and the like, or combinations thereof
  • alkali metal borates
  • alkaline pH modifiers may be suitable for use in the antimicrobial multi-purpose compositions.
  • Commercially available alkaline pH modifiers may include amino alcohols include, but are not limited to, primary amino alcohols (e.g. 2- Amino-2-methyl-l -propanol), amino alcohols (e.g. 2-Amino-2-methyl-l -propanol), commercially available alkyl alkanolamines including, but not limited to, monoethanolamine and triethanolamine.
  • the alkaline pH modifiers can include ethanolamines and/or carbonates fn a further preferred aspect, the alkaline pH modifiers include monoethanolamine, diethanolamine, triethanolamine, 2-amino-2-methyl-l -propanol, monoisopropanolamine, diisopropanolamine, 2-(2-Aminoethoxyl)ethanol (DGA) and/or an alkali metal carbonate fn a further preferred aspect, the alkaline pH modifiers do not include caustic, including for example, any alkali metal hydroxides fn still other preferred aspects, the alkaline pH modifiers do not include monoethanolamine, caustic and/or other highly alkaline components that result in an index value that require classification as a hazardous material, thereby requiring use of personal protective equipment (PPE) when handling the antimicrobial multi purpose composition fn such preferred aspects, the alkaline pH modifiers monoethanolamine, caustic and/or other highly alkaline components are included at less than about
  • PPE personal
  • compositions may include an acidic pH modifier.
  • the acidic pH modifier can be a combination of a weak acid and a strong acid.
  • Strong acids that can be used are acids which substantially dissociate an aqueous solution.
  • "Weak" organic and inorganic acids are acids or acid components in which the first dissociation step of a proton from the acid moiety does not proceed essentially to completion when the acid is dissolved in water at ambient temperatures at a concentration within the range useful to form the present compositions.
  • an acidic pH modifier is believed to affect the lipid envelope and/or capsid in the same manner. Moreover, the acidic pH modifiers disclosed herein facilitate the creation of a low pH buffer on the surface of a substrate, thereby prolonging the residual antimicrobial and antimicrobial activity of the compositions and products in which they are incorporated.
  • Exemplary strong acids suitable for use modifying the pH of the compositions include methane sulfonic acid, sulfuric acid, sodium hydrogen sulfate, phosphoric acid, phosphonic acid, nitric acid, sulfamic acid, hydrochloric acid, trichloroacetic acid, trifluoroacetic acid, toluene sulfonic acid, glutamic acid, and the like; alkane sulfonic acid, such as methane sulfonic acid, ethane sulfonic acid, linear alkyl benzene sulfonic acid, xylene sulfonic acid, cumene sulfonic acid and the like.
  • the compositions include a strong acid having a pKa less than about 2.5 to beneficially provide the acidic use compositions having a pH less than about 4, or preferably less than about 3.
  • the compositions include a strong acid in combination with the anionic surfactant, and optionally include a weak acid.
  • Exemplary weak acids suitable for use modifying the pH of the compositions include alpha hydroxy carboxylic acid, such as lactic acid, citric acid, tartaric acid, malic acid, gluconic acid, and the like; carboxylic acids, such as formic acid, acetic acid, propionic acid and the like; other common organic acids such as ascorbic acid, glutamic acid, levulinic acid, etc. could also be used.
  • the compositions include a weak acid having a pKa greater than about 2.5 to beneficially provide the acidic use compositions having a pH less than about 4, or preferably less than about 3.
  • the compositions include a weak acid in combination with the anionic surfactant, and optionally include a strong acid.
  • the composition is free of mono-carboxylic acids, di-carboxybc acids, or both mono- and di-carboxybc acids.
  • the compositions can contain less than 0.5 wt.%, preferably less than about 0.1 wt.%, more preferably less than about 0.01 wt.%, and most preferably free of a carboxylic acid, a strong acid, a weak acid, a peracid, or mixture thereof.
  • the compositions can comprise an organic solvent.
  • the concentrated antimicrobial multi-purpose composition comprises between about 1 wt.% and about 30 wt.%, more preferably between about 2 wt.% and about 20 wt.%, and most preferably between about 5 wt.% and about 10 wt.% of a solvent.
  • the ready -to-use antimicrobial multi-purpose composition comprises between about 0.01 wt.% and about 2 wt.%, more preferably between about 0.05 wt.% and about 1.5 wt.%, and most preferably between about 0.1 wt.% and about 1 wt.% of a solvent.
  • the solvent is a hydrophobic oxygenated solvent.
  • Exemplary solvents and solvent systems include limited water-solubility alcohols.
  • a benzyl alcohol solvent and/or solvent system is employed.
  • a phenoxy ethanol solvent and/or solvent system is employed.
  • the solvent provides a limited water solubility alcohol providing hydrophobicity that adds affinity towards greasy soils and acts as a plasticizer.
  • the solvent has a solubility in water of preferably less than 15% water soluble, more preferably less than 8 % water soluble, and most preferable less than 5% water soluble.
  • the composition only contains solvent with limited water solubility.
  • the compositions can comprise both a solvent with limited water solubility and also a co-solvent having slightly more water solubility.
  • Additional suitable solvents and solvent systems may include one or more different solvents including aromatic alcohols, ether amines, amidines, esters, glycol ethers, and mixtures thereof.
  • Representative glycol ether solvents may include aromatic glycol ether solvents, such as ethylene glycol phenyl ether (commercially available from Dow as
  • Dowanol Eph or diethylene glycol phenyl ether (commercially available as Dowanol DiEPh).
  • Additional suitable solvents may include l,8-Diazabicyclo[5.4.0]undec-7-ene, or also may be referred to as 2,3,4,6,7,8,9,10-Octahydropyrimidol[l,2-a]azepine (or DBU), 2.5.7.10- tetraoxaundecante (TOU), acetamidophenol, acetanilide, acetophenone, 2-acetyl- 1- methylpyrrole, ethyl hexyl glycerine, benzyl acetate, benzyl alcohol, methyl benzyl alcohol, alpha phenyl ethanol, benzyl benzoate, benzyloxyethanol, ethylene glycol phenyl ether, a propylene glycol, propylene glycol phenyl ether, amyl
  • diethoxyethanol diethylene glycol methyl ether, diisobutyl carbinol, diisobutyl ketone, dimethyl heptanol, dipropylene glycol tert-butyl ether, 2-ethylhexanol, ethyl propionate, ethylene glycol methyl ether acetate, hexanol, isobutanol, isobutyl acetate, isobutyl heptyl ketone, isophorone, isopropanol, isopropyl acetate, methanol, methyl amyl alcohol, methyl n- amyl ketone, 2-methyl- 1 -butanol, methyl ethyl ketone, methyl isobutyl ketone, 1-pentanol, n- pentyl propionate, 1 -propanol, n-propyl acetate, n-propyl propionate, propylene
  • Monoisobutyrate diethylene glycol monohexyl ether, ethylene glycol monohexyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, ethylene glycol methyl ether acetate, ethylene glycol monomethyl ether, dipropylene glycol monomethyl ether, propylene glycol methyl ether acetate, propylene glycol monomethyl ether, diethylene glycol monopropyl ether, ethylene glycol monopropyl ether, dipropylene glycol monopropyl ether and propylene glycol monopropyl ether.
  • Representative dialkyl carbonates include dimethyl carbonate, diethyl carbonate, dipropyl carbonate, diisopropyl carbonate and dibutyl carbonate.
  • Representative oils include benzaldehyde, pinenes (alphas, betas, etc.), terpineols, terpinenes, carvone, cinnamealdehyde, bomeol and its esters, citrals, ionenes, jasmine oil, limonene, dipentene, linalool and its esters.
  • dibasic esters include dimethyl adipate, dimethyl succinate, dimethyl glutarate, dimethyl malonate, diethyl adipate, diethyl succinate, diethyl glutarate, dibutyl succinate, dibutyl glutarate and products available under the trade designations DBE, DBE-3, DBE-4, DBE-5, DBE-6, DBE-9, DBE-IB, and DBE-ME from DuPont Nylon.
  • Representative phthalate esters include dibutyl phthalate, diethylhexyl phthalate and diethyl phthalate. Additional solvents include glycerin and glycerin mono alkyl ethers such as mono heptyl glycerin, and 1,2 alkane diols such as 1,2 octane diol.
  • the solvent is one or more of benzyl alcohol and/or a solvent from the Dowanol E series and/or Dowanol P series.
  • the cleaning compositions When used at an appropriate concentration, which can be indicated by the pH, the cleaning compositions provide antimicrobial efficacy when in contact with a microbial population.
  • the compositions are also effective at removal of soils form a surface.
  • the compositions can be used to clean a surface that is soiled and/or having a microbial population.
  • the methods of use for antimicrobial, including antiviral, disinfection along with inactivating viruses include a contacting step, wherein the antimicrobial multi-purpose compositions disclosed herein are applied to a surface in need of treatment.
  • the contacting may involve contacting the antimicrobial multi-purpose composition with a food contact and/or non-food contact hard surface.
  • a food contact and/or non-food contact hard surface can further include instruments, such as medical instruments. Surfaces can also include those cleaned in third-sink sanitizing, including various wares.
  • contacting the composition can be to a CIP (clean in place) application.
  • contacting the composition may be contacting the composition with a ware wash machine, such as a ware wash application.
  • Such surfaces can include soft surfaces, ware, and/or hard surfaces.
  • Preferred surfaces can comprise one or more of a bath, a carpet, a container, a counter, a curtain, a door, a door handle, a drain, a fabric, a floor, a fluid tank, a hospital partition, a mirror, a monitor, a pipe, a rail, a shower, a sink, a textile, a thermostat, a touch screen, an upholstery, a wall, a window, a woven surface, and a non-woven surface.
  • the various surfaces to which the compositions can be applied can include any conventional application means. Suitable applications can include, for example, by wiping, spraying, pouring, mopping, dipping, immersing, or the like.
  • the contacting step allows the composition to contact the surface for a predetermined amount of time. The amount of time can be sufficient to allow, including from a few seconds to an hour, from about 30 seconds to about 15 minutes, or any range therebetween.
  • the methods may comprise a single step of applying the composition onto the surface without direct physical removal, such as a rinse step.
  • the compositions can be on a wipe such that the wipe can be applied to a surface.
  • the methods can further include a precleaning step, such as where a antimicrobial multi-purpose compositions is applied, wiped and/or rinsed, and thereafter followed by the applying of the compositions.
  • a precleaning step such as where a antimicrobial multi-purpose compositions is applied, wiped and/or rinsed, and thereafter followed by the applying of the compositions.
  • the compositions and methods of use thereof can include treating cleaned or soiled surfaces.
  • Polystyrene resin beads functionalized with chlorine an exemplary substrate commercially available from a variety of sources.
  • Sodium Chloride an ionic salt commercially available from a variety of sources.
  • Sodium Carbonate an alkalinity source commercially available from a variety of sources.
  • Sodium Hydroxide an alkalinity source commercially available from a variety of sources.
  • Reactive Orange 16 Dye An anionic dye belonging to the class of azo dyes.
  • Congo Red Dye A benzidine-based anionic diazo dye.
  • m-Cresol Purple Dye A triarylmethane dye.
  • a cellulose sponge was tested with reactive dye to determine whether the reactive dye could detect changes in pH levels within a cellulose substrate.
  • the cellulose sponge contained a highly alkaline center in comparison to a less alkaline surrounding area of the sponge.
  • the cellulose sponge was saturated with Reactive Orange 16 dye to test its pH indicator abilities. The results are shown in Figure 24.
  • Reactive Orange 16 dye was successful in detecting a pH change on the cellulose sponge substrate.
  • the area of high alkalinity resulted in a visibly darker shade than the surrounding area with a lower pH, indicating that the reactive dye was effective in providing a visual indication of pH change on a cellulose substrate.
  • Reactive dyes were further tested with substrates such as functionalized porous beads to determine whether the dyes would be effective in visually detecting changes in pH.
  • Functionalized porous beads were prepared in test tubes at various pH levels as shown in Table 1. Congo Red dye was then added to each test tube. The results are shown in Figure 25.
  • Reactive dyes were further evaluated for compatibility for use with paint in contemplation of coating substrate surfaces. To test compatibility with various paints, water- based and oil-based paint samples were used. Three paint samples were combined with m- Cresol Purple dye, and an additional three paint samples were combined with Reactive Orange 16. Various dyes were applied to each paint sample to determine whether the dyes would be compatible.
  • the results are shown in Figure 26.
  • the paint samples labeled 1 and 2 were water- based paint, whereas the paint samples labeled 3 were oil-based paint.
  • the dyes that were applied to the water-based paint resulted in distinct colors, indicating that the dyes dissolved and therefore were not compatible with water-based paint.
  • the dyes that were applied to the oil-based paint did not result in a color change, indicating that the dyes did not dissolve and therefore were compatible with oil-based paint.
  • The“colorless” drops were at pH 7 and the drops at the top and darker drops at the bottom were at pH 13.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Physics & Mathematics (AREA)
  • Pathology (AREA)
  • Plasma & Fusion (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Mechanical Engineering (AREA)
  • Molecular Biology (AREA)
  • Biophysics (AREA)
  • Epidemiology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Detergent Compositions (AREA)
  • Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
  • Apparatus For Disinfection Or Sterilisation (AREA)
  • Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
  • Cleaning By Liquid Or Steam (AREA)

Abstract

L'invention concerne des indicateurs colorés sensibles au pH qui indiquent l'efficacité d'une composition de nettoyage pour une activité antimicrobienne en présentant un changement de couleur. En particulier, les indicateurs colorés sensibles au pH comprennent un colorant sensible au pH et un substrat, le colorant étant lié au substrat. Dans un aspect de l'invention, le colorant peut être lié chimiquement, lié physiquement, revêtu sur un substrat, ou peint sur un substrat.
PCT/US2020/032344 2019-05-10 2020-05-11 Indicateur coloré sensible au ph pour des applications de désinfection WO2020231924A1 (fr)

Priority Applications (8)

Application Number Priority Date Filing Date Title
AU2020274035A AU2020274035B2 (en) 2019-05-10 2020-05-11 pH sensitive color indicator for sanitizing applications
CN202080034554.7A CN113811760B (zh) 2019-05-10 2020-05-11 用于消毒应用的pH敏感型颜色指示器
CN202411606159.8A CN119460419A (zh) 2019-05-10 2020-05-11 具有用于消毒应用的pH敏感型颜色指示器的容器
JP2021566479A JP7282919B2 (ja) 2019-05-10 2020-05-11 消毒用途向けのｐＨ感受性色指示薬
EP20729457.0A EP3953702A1 (fr) 2019-05-10 2020-05-11 Indicateur coloré sensible au ph pour des applications de désinfection
MX2021013714A MX2021013714A (es) 2019-05-10 2020-05-11 Indicador de color sensible al ph para aplicaciones de esterilizacion.
EP22178057.0A EP4083621B1 (fr) 2019-05-10 2020-05-11 Indicateur de couleur sensible au ph pour des applications de désinfection
BR112021022415-7A BR112021022415B1 (pt) 2019-05-10 2020-05-11 Indicador sensível a ph, métodos para detectar uma concentração de uma composição de limpeza e para limpar uma superfície, e, recipiente

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201962846144P 2019-05-10 2019-05-10
US62/846,144 2019-05-10

Publications (1)

Publication Number Publication Date
WO2020231924A1 true WO2020231924A1 (fr) 2020-11-19

Family

ID=70919147

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2020/032344 WO2020231924A1 (fr) 2019-05-10 2020-05-11 Indicateur coloré sensible au ph pour des applications de désinfection

Country Status (7)

Country Link
US (2) US12226543B2 (fr)
EP (2) EP3953702A1 (fr)
JP (1) JP7282919B2 (fr)
CN (2) CN113811760B (fr)
AU (1) AU2020274035B2 (fr)
MX (1) MX2021013714A (fr)
WO (1) WO2020231924A1 (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20220080075A1 (en) * 2020-09-11 2022-03-17 Spotcheck, Inc. System and Method for Verifying Cleaning
DE102021204609A1 (de) * 2021-05-06 2022-11-10 FNT-GmbH Verfahren zur Beschichtung von Zinkdruckgussteilen, mehrlagige Beschichtung zum Schutz von Zinkdruckgussteilen und beschichtetes Zinkdruckgussteil
EP4453098A1 (fr) * 2021-12-22 2024-10-30 Ecolab USA Inc. Compositions de résine polymère à changement de couleur
WO2024165161A1 (fr) * 2023-02-09 2024-08-15 V-Zug Ag Procédé de fonctionnement d'un lave-vaisselle utilisant une unité de mesure servant à mesurer une valeur de ph du liquide de lavage
CN116676018B (zh) * 2023-06-16 2024-12-20 山东利尔康医疗科技股份有限公司 一种压力蒸汽灭菌五类指示物油墨配方及其制备方法

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4029598A (en) 1969-03-14 1977-06-14 E. Merck A. G. Non-bleeding indicator and dyes therefor
US20110158917A1 (en) * 2009-12-31 2011-06-30 Macdonald John Gavin Anti-viral tissue product with visual efficacy indicator
US20120093736A1 (en) * 2010-10-15 2012-04-19 Illinois Tool Works Inc. Reversible color-changing ink formulations and nonwoven wipes
WO2016120165A1 (fr) * 2015-01-26 2016-08-04 Novozymes A/S Dosage, procédé, dispositif et nécessaire permettant de détecter des composés odorants

Family Cites Families (102)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1313180A (en) 1970-09-23 1973-04-11 Unilever Ltd Surface active liquids
US3926830A (en) 1970-11-25 1975-12-16 Dainichiswika Color & Chemical Detergent composition having polymer bonded indicator
FR2198991A1 (en) 1972-09-08 1974-04-05 Dainichiseika Color Chem Washing agents contg pH colour indicator - to indicate the pH range over which the surface active agent loses its cleaning capacity
GB1424714A (en) 1973-02-13 1976-02-11 Colgate Palmolive Co Solution dilution indicator
US3930407A (en) 1974-01-07 1976-01-06 Alburger James R Water-washable inspection penetrant employing mineral solvent and a fatty acid solubility promoter
JPS5554898Y2 (fr) 1974-07-24 1980-12-19
JPS6044013B2 (ja) 1975-12-16 1985-10-01 千代田化工建設株式会社 炭化水素類の水素化処理用触媒の製造方法
GB1601922A (en) 1977-03-11 1981-11-04 Minnesota Mining & Mfg Steam formaldehyde sterilization indicator
IE47368B1 (en) 1977-09-27 1984-03-07 Exterma Germ Prod Impreganted substrate
US4532216A (en) 1982-12-27 1985-07-30 Miles Laboratories, Inc. Use of quaternary ammonium polyelectrolyte salts in test means, test device and method for determining the ionic strength or specific gravity of a liquid sample
DE3306225A1 (de) 1983-02-23 1984-08-23 Fritz 7347 Bad Überkingen Stahlecker Vorrichtung zum oe-friktionsspinnen
GB8518736D0 (en) 1985-07-24 1985-08-29 Fibre Treatments Ltd Impregnated substrate
JPH0789114B2 (ja) 1986-04-07 1995-09-27 フマキラー株式会社 間接薬効終点指示体
JPS62261060A (ja) 1986-05-06 1987-11-13 Dainippon Printing Co Ltd ｐＨ測定用インキ組成物および検査体
US4800066A (en) 1986-07-21 1989-01-24 The Drackett Company End of life indicator for automatic toilet cleaning devices
US4855239A (en) 1987-12-28 1989-08-08 Environmental Test Systems, Inc. Test composition and device for the determination of cyanuric acid in water
GB8805500D0 (en) 1988-03-08 1988-04-07 Browne Albert Ltd Temperature disinfection indicator
FR2673640B1 (fr) 1991-03-07 1994-08-19 Reckitt Colman Nouvelles compositions a usage menager, leur procede de preparation et leurs applications notamment dans le domaine de l'entretien menager.
CA2058252A1 (fr) 1991-03-18 1992-09-19 Linda R. Robertson Essai de selection de produit synergiste pour biocides
JPH04291153A (ja) * 1991-03-20 1992-10-15 Jun Kojima 尿検査方法並びに尿検査器具
US5565363A (en) 1991-10-21 1996-10-15 Wako Pure Chemical Industries, Ltd. Reagent composition for measuring ionic strength or specific gravity of aqueous solution samples
US5242602A (en) 1992-03-04 1993-09-07 W. R. Grace & Co.-Conn. Spectrophotometric monitoring of multiple water treatment performance indicators using chemometrics
AU687396B2 (en) 1993-04-28 1998-02-26 Environmental Test Systems, Inc. Method and device for the determination of polymeric biguanides in aqueous fluids
US5523075A (en) 1993-05-13 1996-06-04 Fuerst; Ronnie S. Materials and methods utilizing a temporary visual indicator
US6395551B1 (en) 1994-02-16 2002-05-28 3M Innovative Properties Company Indicator for liquid disinfection or sterilization solutions
JPH0885550A (ja) 1994-09-17 1996-04-02 Kobayashi Uchinuki Kogei Kk バケツ
US5558840A (en) * 1995-07-07 1996-09-24 Jones; Timothy B. Specimen cup holder
US6277646B1 (en) * 1997-05-05 2001-08-21 Dade Behring Inc. Fluid specimen collecting and testing apparatus
JPH10282002A (ja) 1997-03-31 1998-10-23 Sachiyo Hayashi ｐＨ指示薬
US5942438A (en) * 1997-11-07 1999-08-24 Johnson & Johnson Medical, Inc. Chemical indicator for oxidation-type sterilization processes using bleachable dyes
GB9815002D0 (en) 1998-07-11 1998-09-09 Jna Ltd Formulations
US6329207B1 (en) 1999-02-11 2001-12-11 Steris Corporation Wet chemical indicator for the evaluation of peracetic acid chemistries
US20030059483A1 (en) 1999-02-24 2003-03-27 Sowle Eddie D. Color stable hypochlorous sanitizer and methods
MXPA01008617A (es) 1999-02-24 2002-07-30 Kay Chemical Co Sanitizante hipocloroso de color estable y metodos.
US6257440B1 (en) * 1999-04-08 2001-07-10 Ropak Corporation Container handle and related methods
US6410338B1 (en) 1999-05-14 2002-06-25 Ethicon, Inc. Method of indicating an oxidizing agent
CA2375740A1 (fr) 1999-06-09 2000-12-14 Carnegie Mellon University Colorants a base de cyanine sensibles au ph utilises comme reactifs fluorescents
AUPQ747900A0 (en) 2000-05-12 2000-06-08 Novapharm Research (Australia) Pty Ltd Biocidal cloth
DE10046995B4 (de) 2000-09-22 2006-01-05 Henkel Kgaa Reinigungsmittel
FR2816926B1 (fr) * 2000-11-20 2003-02-14 Becton Dickinson France Emballage multifonctionnels, et plus particulierement emballages destines a transporter des produits sterilises ou destines a etre sterilises
US20020110498A1 (en) 2000-12-05 2002-08-15 Jeffrey Dundale Compositions able to indicate when they become inefficient in use
AU2006236076A1 (en) 2001-03-16 2006-12-07 Ethicon, Inc. MBTH for aliphatic aldehyde measurement
US7112448B2 (en) 2001-03-16 2006-09-26 Ethicon, Inc. MBTH for aliphatic aldehyde measurement
US6669908B2 (en) * 2001-07-25 2003-12-30 Applied Biotech, Inc. Urine test device
US20030220213A1 (en) 2002-05-24 2003-11-27 Bober Andrew M. Color changing floor finish stripper
US20040184965A1 (en) * 2003-03-18 2004-09-23 Smith Jack V. Testing cup
GB2408330B (en) 2003-11-22 2008-12-03 Advanced Gel Technology Ltd Polymeric materials comprising pH indicators for use in wound dressings
US7393450B2 (en) 2003-11-26 2008-07-01 Silveri Michael A System for maintaining pH and sanitizing agent levels of water in a water feature
US7282349B2 (en) 2003-12-16 2007-10-16 Kimberly-Clark Worldwide, Inc. Solvatochromatic bacterial detection
DE602005024546D1 (de) 2004-06-15 2010-12-16 Procter & Gamble System zur bewertung des ph-werts und der pufferkapazität von feuchtigkeit enthaltenden reinigungsartikeln
GB2423360A (en) 2005-02-22 2006-08-23 Sun Chemical Ltd Time/Temperature Indicator, Preparation and Use
JP2006308423A (ja) * 2005-04-28 2006-11-09 Chubu Kiresuto Kk ｐＨ変色指示性繊維およびその製法、並びにそれを用いたｐＨ検知法、ｐＨ検知システム、ｐＨ検知器
US20060293205A1 (en) * 2005-06-27 2006-12-28 Jessica Chung Cleaning substrate with a visual cue
US8481331B2 (en) 2005-09-08 2013-07-09 American Sterilizer Company Oxidative dye composition and indicator
US7807473B2 (en) 2005-10-26 2010-10-05 General Electric Company Material compositions for sensors for determination of chemical species at trace concentrations and method of using sensors
WO2007054238A1 (fr) 2005-11-08 2007-05-18 Unilever N.V. Dispositif indicateur d'hygiene
WO2007070649A2 (fr) 2005-12-14 2007-06-21 3M Innovative Properties Company Systeme de revetement anti-microbien
IL176170A0 (en) * 2006-06-07 2006-10-05 Curver Luxembourg Sarl Mop bucket
WO2008006154A1 (fr) 2006-07-11 2008-01-17 Paul Nigel Brockwell Dispositif indicateur de l'état de santé et procédé associé
WO2008074635A1 (fr) 2006-12-20 2008-06-26 Unilever Plc Composition de détergent pour le linge
US20080223413A1 (en) 2007-03-14 2008-09-18 Radford Philip T Color changing soap
JP4901592B2 (ja) 2007-05-14 2012-03-21 東洋製薬化成株式会社 アルデヒド系消毒剤の有効濃度判定用固形剤型インディケータ
US8071390B2 (en) 2007-06-05 2011-12-06 Ecolab Usa Inc. Temperature stabilized optical cell and method
WO2009005936A1 (fr) 2007-06-29 2009-01-08 3M Innovative Properties Company Accélération d'une réaction avec la ninhydrine
US8343908B2 (en) 2007-07-12 2013-01-01 Kimberly-Clark Worldwide, Inc. Foaming hand sponge with color change indicator
US8440606B2 (en) 2007-07-12 2013-05-14 Kimberly-Clark Worldwide, Inc. Foaming hand sponge for bodily cleansing with color change indicator
JP2010538101A (ja) 2007-08-31 2010-12-09 ザ プロクター アンド ギャンブル カンパニー 組成物及び視覚認識変化方法
US20090093063A1 (en) 2007-09-07 2009-04-09 Anslyn Eric V Color Changing and Coverage Indicating Hand Sanitizer
EP2060622A1 (fr) 2007-11-13 2009-05-20 The Procter & Gamble Company Composition de nettoyage de surface dure
US20090185956A1 (en) 2008-01-18 2009-07-23 Michael Carl Junger pH SENSITIVE INDICATOR DEVICE
FR2931836B1 (fr) 2008-06-02 2011-01-21 Victor Seita Decapant nettoyant acide avec indicateur visuel de dosage et temoin de rincage
US8772184B2 (en) 2009-03-31 2014-07-08 Illinois Tool Works Inc. Reversible color-changing sanitizer-indicating nonwoven wipe
CN102803504B (zh) 2009-06-15 2015-07-01 3M创新有限公司 产酸菌的检测
US20110003391A1 (en) * 2009-07-02 2011-01-06 Scott Martell Boyette Sensor films, methods for making and methods for monitoring water-soluble polymer concentrations
CN201434787Y (zh) 2009-07-09 2010-03-31 山东省千佛山医院 一种留取尿标本专用桶
US8839975B2 (en) * 2009-08-03 2014-09-23 Ropak Corporation Container and lid
DE102009050798A1 (de) 2009-10-27 2011-04-28 Langhals, Heinz, Prof. Dr. Micellare Nano-Fluoreszenzindikatoren
JP5116048B2 (ja) 2010-03-10 2013-01-09 独立行政法人科学技術振興機構 触媒および反応方法
JP2012029770A (ja) 2010-07-29 2012-02-16 Rengo Co Ltd 二酸化塩素製剤インジケータ
WO2012016350A1 (fr) 2010-08-03 2012-02-09 General Electric Company Détermination simultanée de multiples analytes dans un système de distribution d'eau industriel
PL215147B1 (pl) 2010-12-13 2013-10-31 Univ West Pomeranian Szczecin Tech Sposób oznaczania zawartości środków kationowo czynnych metodą dwufazowego miareczkowania bezpośredniego
US9341613B2 (en) * 2011-02-07 2016-05-17 Kevin G. Sawa Device for singulating and dispensing rigid and semi-rigid strips
US20120208733A1 (en) 2011-02-14 2012-08-16 Adam Quarles Soap Scum Indicating Cleaning Composition
US9144620B2 (en) * 2011-09-09 2015-09-29 Ecolab Usa Inc. Real time indicator for quaternary ammonium compound concentration
US9295613B2 (en) 2011-12-13 2016-03-29 Fenwal, Inc. Container with pH indicator
WO2013184182A1 (fr) 2012-06-05 2013-12-12 Ecolab Usa Inc. Capteur optique permettant de déterminer la concentration en un composé d'ammonium quaternaire
WO2014102556A1 (fr) 2012-12-27 2014-07-03 Ideapool Kft. Récipient avec dispositif d'indication
EP2764776A1 (fr) 2013-02-07 2014-08-13 Thonhauser GmbH Détection de salissures de surfaces
US9949724B2 (en) * 2013-02-22 2018-04-24 Instant Tech Subsidiary Acquisition Inc. Specimen cup including test card slot and method of use thereof
JP6073728B2 (ja) 2013-03-28 2017-02-01 株式会社安藤・間 腐蝕抑制剤の簡易検知方法、並びに腐蝕抑制剤の簡易検知組成物及び簡易検知キット
US9170205B2 (en) 2013-09-18 2015-10-27 Metrex Research, LLC Disinfection and cleaning confirmation system
DE102013226512A1 (de) 2013-12-18 2015-06-18 Henkel Ag & Co. Kgaa Einweg-Spülpad
JP6023764B2 (ja) 2014-08-25 2016-11-09 日本電信電話株式会社 不整合検出装置及び不整合検出方法
KR101605193B1 (ko) 2014-11-26 2016-03-29 (주)지피엔이 친환경 습도지시제 및 이를 이용한 습도지시키트
WO2016090469A1 (fr) 2014-12-08 2016-06-16 Dalhousie University Distributeur améliorant l'hygiène
WO2016161247A1 (fr) 2015-04-02 2016-10-06 Ecolab Usa Inc. Procédé destiné à mesurer la concentration de polymères dans des systèmes d'eau
EP3346836B1 (fr) 2015-09-10 2021-07-21 Ecolab USA Inc. Produit chimique antimicrobien auto-indicateur
EP3420098A1 (fr) 2016-02-23 2019-01-02 Koninklijke Philips N.V. Procédé de détection in situ d'altération de lait maternel
WO2017205474A1 (fr) 2016-05-24 2017-11-30 Smartwash Solutions, Llc Procédé et système de gestion de l'eau dans un bac de préparation d'aliments
KR101923815B1 (ko) 2017-03-22 2018-11-29 국방과학연구소 색도 측정을 이용한 미생물 농도 측정 방법
AU2018275185B2 (en) 2017-05-29 2023-01-05 Dow Global Technologies Llc A hard surface cleaning composition and method of using same
US20200138021A1 (en) 2017-07-14 2020-05-07 Spongebath Llc Cleaning and Antimicrobial Composition and Its Uses

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4029598A (en) 1969-03-14 1977-06-14 E. Merck A. G. Non-bleeding indicator and dyes therefor
US20110158917A1 (en) * 2009-12-31 2011-06-30 Macdonald John Gavin Anti-viral tissue product with visual efficacy indicator
US20120093736A1 (en) * 2010-10-15 2012-04-19 Illinois Tool Works Inc. Reversible color-changing ink formulations and nonwoven wipes
WO2016120165A1 (fr) * 2015-01-26 2016-08-04 Novozymes A/S Dosage, procédé, dispositif et nécessaire permettant de détecter des composés odorants

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
"Official Methods of Analysis of the Association of Official Analytical Chemists", 1990, article "Germicidal and Detergent Sanitizing Action of Disinfectants"
See also references of EP3953702A1

Also Published As

Publication number Publication date
EP4083621B1 (fr) 2025-05-14
AU2020274035A1 (en) 2021-11-25
CN113811760A (zh) 2021-12-17
EP3953702A1 (fr) 2022-02-16
US20250152767A1 (en) 2025-05-15
JP2022532165A (ja) 2022-07-13
EP4083621A1 (fr) 2022-11-02
BR112021022415A2 (pt) 2021-12-28
US20200353118A1 (en) 2020-11-12
CN119460419A (zh) 2025-02-18
AU2020274035B2 (en) 2023-02-02
MX2021013714A (es) 2021-12-10
US12226543B2 (en) 2025-02-18
CN113811760B (zh) 2024-11-15
JP7282919B2 (ja) 2023-05-29

Similar Documents

Publication Publication Date Title
AU2020274035B2 (en) pH sensitive color indicator for sanitizing applications
AU2023201139B2 (en) Antimicrobial multi-purpose cleaner and methods of making and using the same
AU2020271558B2 (en) Hard surface cleaning solution with rapid viricidal activity
CA2565814C (fr) Systeme de decontamination pour instruments medicaux
AU2017217521B2 (en) Method and composition for rapid detection of protein soils
EA025614B1 (ru) Микробицидная композиция
BR112021022415B1 (pt) Indicador sensível a ph, métodos para detectar uma concentração de uma composição de limpeza e para limpar uma superfície, e, recipiente
EA025499B1 (ru) Микробицидная композиция
US20240424159A1 (en) Cellulosic fiber blends for disinfecting wipes with improved tear strength

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 20729457

Country of ref document: EP

Kind code of ref document: A1

DPE1 Request for preliminary examination filed after expiration of 19th month from priority date (pct application filed from 20040101)
ENP Entry into the national phase

Ref document number: 2021566479

Country of ref document: JP

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

REG Reference to national code

Ref country code: BR

Ref legal event code: B01A

Ref document number: 112021022415

Country of ref document: BR

ENP Entry into the national phase

Ref document number: 2020274035

Country of ref document: AU

Date of ref document: 20200511

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: 2020729457

Country of ref document: EP

Effective date: 20211108

ENP Entry into the national phase

Ref document number: 112021022415

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20211108